Visualization of latent fingerprint corrosion of metallic surfaces

Abstract:  Chemical reactions between latent fingerprints and a variety of metal surfaces are investigated by heating the metal up to temperatures of ∼600°C after deposition of the fingerprint. Ionic salts present in the fingerprint residue corrode the metal surface to produce an image of the fingerprint that is both durable and resistant to cleaning of the metal. The degree of fingerprint enhancement appears independent of the elapsed time between deposition and heating but is very dependent on both the composition of the metal and the level of salt secretion by the fingerprint donor. Results are presented that show practical applications for the enhancement to fingerprints deposited in arson crime scenes, contaminated by spray painting, or deposited on brass cartridge cases prior to discharge. The corrosion of the metal surface is further exploited by the demonstration of a novel technique for fingerprint enhancement based on the electrostatic charging of the metal and then the preferential adherence of a metallic powder to the corroded part of the metal surface.     

Can the RUVIS Reflected UV Imaging System Visualize Fingerprint Corrosion on Brass Cartridge Casings Postfiring?

Comparisons are made between the visualization of fingerprint corrosion ridge detail on fired brass cartridge casings, where fingerprint sweat was deposited prefiring, using both ultraviolet (UV) and visible (natural daylight) light sources. A reflected ultraviolet imaging system (RUVIS), normally used for visualizing latent fingerprint sweat deposits, is compared with optical interference and digital color mapping of visible light, the latter using apparatus constructed to easily enable selection of the optimum viewing angle. Results show that reflected UV, with a monochromatic UV source of 254 nm, was unable to visualize fingerprint ridge detail on any of 12 casings analyzed, whereas optical interference and digital color mapping using natural daylight yielded ridge detail on three casings. Reasons for the lack of success with RUVIS are discussed in terms of the variation in thickness of the thin film of metal oxide corrosion and absorption wavelengths for the corrosion products of brass.     

Latent Fingerprint Visualization using a Scanning Kelvin Probe in Conjunction with Vacuum Metal Deposition

The application of vacuum metal deposition before scanning Kelvin probe visualization of fingerprints is investigated. The potential contrast between fingerprint ridges and furrows is maximized by the use of silver deposition for non‐noble metals and gold–zinc deposition for noble metals. The higher susceptibility of eccrine fingerprints to vacuum metal overdeposition is confirmed. Additionally, fingerprints are best developed individually and by building the metal deposition slowly to protect against overdevelopment and variation in the rate of metal condensation. The progress of the metal deposition can be monitored using the scanning Kelvin probe by reference to the change in potential and continuity of the new potential on the surface. The use of acetic acid solution for the recovery of overVMD‐developed samples is shown not to be useful. Applying the metal deposition has the additional prospect of increasing surface conductivity and homogeneity and both can aid fingerprint visualization using the scanning Kelvin probe.     

A Comparison of Cleaning Regimes for the Effective Removal of Fingerprint Deposits from Brass

Abstract:  Effective removal of fingerprint deposits is crucial for experimentation related to the corrosion of metals by fingerprint deposits. Such removal is also necessary prior to deposition of test fingerprints. The effectiveness of four regimes in removing fingerprint deposits from brass is considered. Sustained wiping of the deposit with a tissue at applied pressures of up to c . 1430 Pa or rubbing while the brass was immersed in acetone both failed to remove completely all traces of fingerprint deposits. Heating the brass to 600°C was an effective remover; however, this also oxidized the surface of the metal except where inhibited by fingerprint deposits. The most effective regime, and the only one of the four that removed all traces of deposit without affecting the properties of the metal surface, was immersion in warm soapy water while rubbing with a tissue. We propose this as the preferred method for fingerprint removal.     

Visualization of Latent Fingerprint Corrosion of Brass

Abstract:  Visualization of latent fingerprint deposits on metals by enhancing the fingerprint-induced corrosion is now an established technique. However, the corrosion mechanism itself is less well understood. Here, we describe the apparatus constructed to measure the spatial variation (Δ V ) in applied potential ( V ) over the surface of brass disks corroded by latent fingerprint deposits. Measurement of Δ V for potential of 1400 V has enabled visualization of fingerprint ridges and characteristics in terms of this potential difference with Δ V typically of a few volts. This visualization is consistent with the formation of a Schottky barrier at the brass-corrosion product junction. Measurement of the work function of the corroded brass of up to 4.87 ± 0.03 eV supports previous results that suggested that the corrosion product is composed of p-type copper oxides. A model for the galvanic corrosion of brass by ionic salts present in fingerprint deposits is proposed that is consistent with these experimental results.     

Visualisation of fingermarks and grab impressions on dark fabrics using silver vacuum metal deposition

Vacuum metal deposition (VMD) involves the thermal evaporation of metal (silver) in a vacuum, resulting in a uniform layer being deposited on the specimen being treated. This paper examines the use of silver on dark fabrics, thus offering a simpler operation and more obvious colouration to that of the traditional use of gold and zinc metals which must be evaporated separately. The aim of this study was to investigate the effect of fabric type, donor, mark age and method of fingermark deposition on the quality of marks visualised using silver VMD. This was achieved by collecting fingermark deposits from fifteen donors, of both sexes and various ages, by a grab or a press method. Four different fabrics: satin, polyester, polycotton and cotton were studied over a 10 day timeline of 1, 2, 3, 4, 5, 6, 7, 14, 21 and 28 + days. It was found that satin and polyester gave the most positive results, with polyester often producing excellent ridge detail. Cotton and polycotton were less successful with no ridge detail being observed. The donors also had an observable effect on the results obtained probably due to variations in secretions produced or pressures applied during specimen collection. The age of the mark or the method of mark deposition had little influence on the results obtained. Silver VMD is a viable process for visualising marks on certain dark fabrics and has the advantage over gold/zinc VMD in that the marks visualised are light in colour which contrasts well against the dark background.     

High Resolution Imaging of Latent Fingerprints by Localized Corrosion on Brass Surfaces

Abstract:  The Atomic Force Microscope (AFM) is capable of imaging fingerprint ridges on polished brass substrates at an unprecedented level of detail. While exposure to elevated humidity at ambient or slightly raised temperatures does not change the image appreciably, subsequent brief heating in a flame results in complete loss of the sweat deposit and the appearance of pits and trenches. Localized elemental analysis (using EDAX, coupled with SEM imaging) shows the presence of the constituents of salt in the initial deposits. Together with water and atmospheric oxygen—and with thermal enhancement—these are capable of driving a surface corrosion process. This process is sufficiently localized that it has the potential to generate a durable negative topographical image of the fingerprint. AFM examination of surface regions between ridges revealed small deposits (probably microscopic "spatter" of sweat components or transferred particulates) that may ultimately limit the level of ridge detail analysis.     

Latent fingerprint detection using a scanning Kelvin microprobe

Electrochemical interactions between latent human fingerprints and metal surfaces in ambient air are investigated using a scanning Kelvin microprobe. Inorganic salts present in sweat deposited at fingerprint ridges locally depassivate the metal surface producing a Volta potential decrease of greater than 200 mV. Volta potential patterns may persist for months and prints may be visualized by potential mapping, even when overcoated with a polymer layer. Because the Volta potential differences are produced by involatile salts they persist when the organic components of the fingerprint residue have been volatilized by heating to 600 degrees C.     

Role of Nanomaterials for Forensic Investigation and Latent Fingerprinting—A Review

The imminent nanotechnology and progressive instrumentations together have vast applications in the field of forensic science. Few prominent examples are gold nanoparticles for improvising the efficiency of polymerase chain reaction and atomic force microscopy for examining ink and bloodstains. Characteristics like distinct ridge details of fingerprints could be obtained by applying different nanoparticles such as silver, zinc oxide, silicon dioxide, aluminum oxide, gold (with silver physical developer), europium, fluorescent carbon, and amphiphilic silica on a range of object surfaces, and among all, gold is most commonly used. Fingerprint is considered noteworthy evidence in any crime scene, and nano-based techniques hold immense future potential in fingerprint investigations. Therefore, this paper focuses on the applications of nanoparticles in developing and detecting the latent fingerprints.     

The quantification of fingerprint quality using a relative contrast index

Research into fingermark enhancement techniques has traditionally used visual comparisons and qualitative methods to assess their effectiveness based on the quality of the developed fingermark. However, with increasing research into the optimisation of these techniques the need for a quantitative evaluative method has arisen. Parameters for acceptable fingerprint quality are not well defined and generally encompass clear, sharp edges and high levels of contrast between the fingermark ridges and background material. Using these current parameters, a conclusive measurement of fingerprint quality and thus the effectiveness of development techniques cannot be achieved.This study presents a model through which an aspect of fingerprint quality can be objectively and impartially measured based on a relative contrast index, constructed through measuring the reflective intensity of the fingermark ridges against the background material. Using a fibre-optic spectrophotometer attached to a microscope with axial illumination, the intensity counts of the ridge detail and background material were measured and a logarithmic contrast index constructed. The microscope and spectrophotometer parameters were experimentally tested using a standard colour resolution chart with known reflective properties. The protocol was successfully applied to four sample groups: black inked fingerprints on white paper; latent fingermarks on white paper developed separately with ninhydrin and physical developer; and fingermarks in blood deposited on white tiles and enhanced with amido black. The contrast indices obtained quantitatively reflect the level of contrast and provide an indication of fingerprint quality through a numerical representation rather than previous qualitative methods. It has been suggested that the proposed method of fingerprint quantification may be viable for application in the forensic research arena as it allows the definitive measurement of contrast to aid the evaluation of fingermark detection and enhancement techniques.     

Visualization of Latent Fingerprint Corrosion on a Discharged Brass Shell Casing

Abstract:  Latent fingerprint visualization on discharged shell casings can provide good forensic evidence, particularly if the casing is recovered at the scene of a crime where a firearm has been discharged. Unfortunately, visualization of such latent fingerprints when they were deposited prior to discharge of the firearm is problematic as both increased temperature and abrasive friction can inhibit fingerprint visualization with conventional techniques. We present a case study that demonstrates latent fingerprint visualization on a discharged shell casing recovered 14 years ago from the scene of a homicide. Previous cyanoacrylate fuming of the casing had failed to reveal any fingerprints. We use a visualization technique in which a conducting carbon powder adheres preferentially to latent fingerprint corrosion of the casing surface, following the application of a potential of 2.5 kV to the casing. This technique presents opportunities for the review of old cases and for consideration of its use in current cases.     

Exploration of the use of novel SiO2 nanocomposites doped with fluorescent Eu3+/sensitizer complex for latent fingerprint detection

Silicon dioxide-based nanocomposites have shown great potential in novel chemical and biological sensor development due to their large loading capacity and high surface area to volume ratio for trapping molecular complexes of various sizes. However, their potential applications in forensic science, latent fingerprint detection in particular, were still unclear. In this study, we have succeeded in trapping the highly fluorescent and photo-stable Eu3+ metal ions/sensitizer complex in silicon dioxide-based nanocomposites, doped xerogels, using the sol-gel method. We have tested the spectroscopic properties of Eu3+ in several combinations of rare earth sensitizers and different derivatives of silicon dioxide nanoporous templates. Our results indicated that the use of 1,10-phenanthroline (OP) sensitizer in tetraethoxysilane (TEOS) template provides the best fluorescently doped xerogels applicable for latent fingerprint detections on various forensic relevant materials, including metal foil, glass, plastic, colored paper, and a green tree leaf. The fabrication procedure, UV/vis and fluorescence characterizations, and fingerprint labeling results of these new Eu3+/OP/TEOS nanocomposites are presented in this exploratory study.     

A simple histochemical technique for the identification of gunshot residue

Alizarin red S (ARS) is a commonly used organic dye useful in the histologic identification of calcium deposits. ARS also forms colored reaction products with other metal ions, including barium and lead, which are present in primer residue. In histochemical studies, ARS is shown to identify primer residues from several manufacturers as well as primer residue deposited in tissue, either experimentally or in close-range gunshot wounds. This can be easily accomplished with routine histologic techniques. ARS does not stain gunpowder residue, tattoo pigment, melanin, graphite, india ink, or anthracotic pigment.     

Development of a GC-MS method for the simultaneous analysis of latent fingerprint components

Latent fingerprint residue is a complex mixture of organic and inorganic compounds. A full understanding of the composition of this mixture and how it changes after deposition is lacking. Three solvent systems were compared for the simultaneous extraction and derivatization with ethyl chloroformate of selected amino and fatty acids from a nonporous substrate (Mylar for subsequent analysis by gas chromatography-mass spectrometry. A solvent system comprised of sodium hydroxide, ethanol, and pyridine was found to be the most effective. This method was applied to the analysis of latent fingerprint residue deposited on Mylar and preliminary data are presented. Twelve amino acids (e.g., serine, glycine, and aspartic acid) and 10 fatty acids (e.g., tetradecanoic, hexadecanoic, and octadecanoic acids) were identified. The potential application of this method to further the understanding of latent fingerprint chemistry has been demonstrated.     

The influence of polymer type, print donor and age on the quality of fingerprints developed on plastic substrates using vacuum metal deposition.

This study investigated fingerprint development on five different polymer substrates using vacuum metal deposition (VMD). The conditions required for optimum development are shown to depend on a number of factors. No one set of conditions will result in good development in all situations. Polymer type has been confirmed as a major factor in determining the types of development that will occur and the optimum VMD conditions required. For more consistently successful VMD development, polymer type should be determined before selecting conditions. While polymer type is a key factor in determining optimum development conditions, there may be variation of the optimum conditions within a polymer type, most likely due to the presence of additives in the plastic. The heaviness of a latent print, i.e. amount of residue that constitutes the print, also affects the VMD conditions required. The donor, manner of deposition, and age of a print affect the heaviness of the deposit. The heavier the print, the higher the gold count necessary for successful VMD development. The occurrence of 'empty prints' (i.e. zinc deposition on the general background but not on or between the print ridges) was found to be related to polymer type and print heaviness. Heavy prints on PVC and PET are the most likely to be 'empty' after VMD treatment. The development of empty prints may be due to the diffusion of print residue into the print valleys. Pre-treatment with cyanoacrylate fuming was also found to affect VMD development. In particular, it was shown that cyanoacrylate pre-treatment was beneficial for print development on PET and PVC. The results of this study were used to formulate guidelines for use as an aid by laboratories using VMD in casework.     

Visualization of latent fingermark corrosion of brass, climatic influence in a comparison between the U.K. and Iraq

Through a comparison of fingermark sweat corrosion of α phase brass in both the U.K. and Iraq, we show how samples from Iraq have improved fingermark corrosion over U.K. samples that require no additional enhancement prior to visualization. Over 50% of Iraqi samples produced fingermark corrosion with full ridge detail compared with 0% from the U.K. X-ray photoelectron spectroscopy analysis of the fingermark corrosion products showed that Iraqi samples exhibit more dezincification with the Zn:Cu ratio averaging 1:1.82 compared with 1:3.07 for U.K. samples. Auger spectroscopy showed the presence of both zinc oxide and copper (I) oxide. No copper (II) was observed on the surface of the corroded brass. Opportunities to exploit the optical properties of these thin film oxides to enhance the visualization of fingermark corrosion are considered, and the potential to use fingermark corrosion of metal as a means of visualizing fingerprints in war zones is discussed.     

Vacuum metal deposition: factors affecting normal and reverse development of latent fingerprints on polyethylene substrates

Vacuum metal deposition (VMD) is an established technique for the development of latent fingerprints on non-porous surfaces. VMD has advantages over cyanoacrylate fuming, especially in circumstances where prints are old, have been exposed to adverse environmental conditions, or are present on semi-porous surfaces. Under normal circumstances, VMD produces 'negative' prints as zinc deposits onto the background substrate and not the print ridges themselves. A phenomenon of 'reverse' development, when zinc deposits onto the print ridges and not the background, has been reported by many authors but its causes have not been conclusively identified.Four plastic substrates were used in this study and these could be easily divided into two groups based on the types of development observed as the amount of deposited gold was increased. On group I plastics, identified as low-density polyethylene (LDPE), normal development then reverse development and finally no development resulted with increasing gold. On group II plastics, identified as high-density polyethylene (HDPE), normal development then over-development and finally poor-quality normal development resulted with increasing gold. Our results suggest that the difference between these plastic types causes variations in the gold film structure which in turn dictates the nature of the zinc deposition.On group I plastics, the structure and thickness of the gold film has been identified as the critical factor in the occurrence of normal or reverse development. Thin gold films on plastic substrates form small 'clusters' (or agglomerates) rather than the atoms being uniformly spread over the surface. The size and shape of these clusters is critical. Once the clusters reach a certain morphology, they no longer act as nucleation sites for zinc, and hence, zinc will not deposit onto the substrate.On group II plastics, results suggest that the gold clusters are smaller and more densely packed. Hence, even though the same amount of gold has been deposited, the gold clusters in this case do not reach the critical morphology and so continue to act as nucleation sites for zinc.Typically, zinc will not deposit onto the fingerprint ridges as the gold nucleation sites are buried within the print residue. However, when more gold is deposited, gold emerges at the surface of the latent print allowing zinc deposition onto the ridges.The rate of gold evaporation was found not to affect the structure of the gold film, although a slower rate of evaporation resulted in more effective deposition.     

Understanding the chemistry of the development of latent fingerprints by superglue fuming

Cyanoacrylate fuming is a widely used forensic tool for the development of latent fingerprints, however the mechanistic details of the reaction between the fingerprint residue and the cyanoacrylate vapor are not well understood. Here the polymerization of ethyl-cyanoacrylate vapor by sodium lactate or alanine solutions, two of the major components in fingerprint residue, has been examined by monitoring the time dependence of the mass uptake and resultant polymer molecular weight characteristics. This data provides insight into the molecular level actions in the efficient development of latent fingerprints by superglue fuming. The results show that the carboxylate moiety is the primary initiator of the polymerization process and that a basic environment inhibits chain termination while an acidic environment promotes it. The results also indicate that water cannot be the primary initiator in this forensic technique.     

Exposing latent fingermarks on problematic metal surfaces using time of flight secondary ion mass spectroscopy

Fingermarks are a key form of physical evidence for identifying persons of interest and linking them to the scene of a crime. Visualising latent (hidden) fingermarks can be difficult and the correct choice of techniques is essential to develop and preserve any fingermarks or other (e.g. DNA) evidence that might be present. Metal surfaces (stainless steel in particular) have proven to be challenging substrates from which to reliably obtain fingermarks. This is a great cause for concern among police forces around the globe as many of the firearms, knives and other metal weapons used in violent crime are potentially valuable sources of fingermark evidence. In this study, a highly sensitive and non-destructive surface science technique called time of flight secondary ion mass spectroscopy (ToF-SIMS) was used to image fingermarks on metal surfaces. This technique was compared to a conventional superglue based fuming technique that was accompanied by a series of contrast enhancing dyes (basic yellow 40 (BY40), crystal violet (CV) and sudan black (SB)) on three different metal surfaces. The conventional techniques showed little to no evidence of fingermarks being present on the metal surfaces after a few days. However, ToF-SIMS revealed fingermarks on the same and similar substrates with an exceptional level of detail. The ToF-SIMS images demonstrated clear ridge definition as well as detail about sweat pore position and shape. All structures were found to persist for over 26?days after deposition when the samples were stored under ambient conditions.     

Diimide-enhanced fingerprint detection with photoluminescent CdS/dendrimer nanocomposites

The chemical development of latent fingerprints by nanocomposites that involve photoluminescent cadmium sulfide nanoparticle aggregates with Starburst dendrimer is demonstrated. The dendrimer bonds to fingerprint residue via its terminal functional groups. When these are amino groups (generation 4 dendrimer), the binding is enhanced by fingerprint pre-treatment with diimide. The diimide converts carboxylic acid moieties of the fingerprint residue to esters that then react with the dendrimer amino groups to form amide linkages. The cadmium sulfide/generation 4 dendrimer development of fingerprints is enhanced by elevated temperature also. Finally, fingerprint development with carboxylate-functionalized cadmium sulfide/generation 3.5 dendrimer nanocomposites is examined. Here, diimide treatment of the dendrimer itself aids the subsequent fingerprint labeling, which involves amino acid of the figerprint residue. Nanocomposite fingerprint detection is compatible with time-resolved imaging for background fluorescence elimination.